ArticleEndocrine oncology (Bristol, England)2023
Clinical presentation of sporadic and hereditary pheochromocytoma/paraganglioma.
Article in Endocrine oncology (Bristol, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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4 citing papers in PubMed, 4 citations in OpenAlex.
- Gallbladder Cancer Concomitant With Para-Aortic Paraganglioma: A Case Report.Clinical case reports · 2025Article
- Genetic landscape of Romanian PPGLs.Journal of cellular and molecular medicine · 2024Article
- Clinical and Genetic Correlation in Neurocristopathies: Bridging a Precision Medicine Gap.Journal of clinical medicine · 2024Review
- Bilateral pheochromocytomas: clinical presentation and morbidity rate related to surgery technique and genetic status.Endocrine connections · 2024Article
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Authors and funding
10 authors at 3 institutions in 2 countries.
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Abstract
Pheochromocytomas (PHEO) and paragangliomas (PGL) can occur sporadic or within genetic predisposition syndromes. Despite shared embryology, there are important differences between PHEO and PGL. The aim of this study was to describe the clinical presentation and disease characteristics of PHEO/PGL. A retrospective analysis of consecutively registered patients diagnosed with or treated for PHEO/PGL in a tertiary care centre was performed. Patients were compared according to anatomic location (PHEO vs PGL) and genetic status (sporadic vs hereditary). In total, we identified 38 women and 29 men, aged 50 ± 19 years. Of these, 42 (63%) had PHEO, and 25 (37%) had PGL. Patients with PHEO presented more frequently with sporadic than hereditary disease (45 years vs 27 (77%) vs 8 (23%)) than patients with PGL (9 (36%) vs 16 (64%), respectively) and were older at diagnosis (55 ± 17 vs 40 ± 18 years,
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